Shen K Z, Cox B A, Johnson S W
Department of Physiology and Pharmacology, Oregon Health Sciences University, Portland 97201, U.S.A.
Neuroscience. 1997 Aug;79(3):649-58. doi: 10.1016/s0306-4522(97)00024-9.
Effects of L-arginine in the nervous system are often attributed to nitric oxide. Using whole-cell patch pipettes to record membrane currents in voltage-clamp from dopamine neurons in the rat midbrain slice, the present studies found that L-arginine potentiates GABA-dependent membrane currents via a nitric oxide-independent mechanism. L-Arginine (0.3-10 mM) increased the peak amplitude, half-width duration and time constant of decay of GABA(B) receptor-mediated inhibitory postsynaptic currents in a concentration-dependent manner. In the presence of CGP 35348 (300 microM), a GABA(B) receptor antagonist, L-arginine also prolonged the duration of inhibitory postsynaptic currents mediated by GABA(A) receptors, but their amplitudes were reduced. L-Arginine (10 mM) also evoked 17+/-3 pA of outward current (at -60 mV) which was significantly increased in the presence of exogenous GABA (100 microM). Pressure-ejection of GABA from micropipettes produced outward currents mediated by GABA(B) receptors (recorded in bicuculline) or GABA(A) receptors (recorded in CGP 35348); both types of receptor-mediated currents were increased by L-arginine (10 mM). In contrast, outward currents evoked by baclofen, a GABA(B) receptor agonist, were not potentiated by L-arginine. The GABA transport inhibitors NO 711 (1 microM) and nipecotic acid (1 mM) significantly increased the half-width duration and time-constant of decay of GABA(B)-mediated inhibitory postsynaptic currents, thus mimicking effects of L-arginine. However, nitric oxide donors failed to mimic effects of L-arginine on GABA(B) inhibitory postsynaptic currents, and inhibitors of nitric oxide synthesis failed to selectively block the action of L-arginine. These findings suggest that L-arginine potentiates GABA synaptic transmission by a nitric oxide-independent mechanism. Similarities between effects of L-arginine, NO 711 and nipecotic acid suggest that L-arginine inhibits a GABA transporter.
L-精氨酸在神经系统中的作用通常归因于一氧化氮。本研究使用全细胞膜片钳记录大鼠中脑切片中多巴胺能神经元在电压钳模式下的膜电流,发现L-精氨酸通过一种不依赖一氧化氮的机制增强GABA依赖性膜电流。L-精氨酸(0.3 - 10 mM)以浓度依赖性方式增加GABA(B)受体介导的抑制性突触后电流的峰值幅度、半峰宽持续时间和衰减时间常数。在GABA(B)受体拮抗剂CGP 35348(300 microM)存在的情况下,L-精氨酸还延长了GABA(A)受体介导的抑制性突触后电流的持续时间,但其幅度减小。L-精氨酸(10 mM)在-60 mV时还诱发了17±3 pA的外向电流,在外源性GABA(100 microM)存在时该电流显著增加。从微量移液器压力喷射GABA产生由GABA(B)受体介导的外向电流(在荷包牡丹碱存在下记录)或由GABA(A)受体介导的外向电流(在CGP 35348存在下记录);两种类型的受体介导电流均被L-精氨酸(10 mM)增强。相比之下,GABA(B)受体激动剂巴氯芬诱发的外向电流未被L-精氨酸增强。GABA转运体抑制剂NO 711(1 microM)和尼克酸(1 mM)显著增加了GABA(B)介导的抑制性突触后电流的半峰宽持续时间和衰减时间常数,从而模拟了L-精氨酸的作用。然而,一氧化氮供体未能模拟L-精氨酸对GABA(B)抑制性突触后电流的作用,一氧化氮合成抑制剂也未能选择性阻断L-精氨酸的作用。这些发现表明,L-精氨酸通过一种不依赖一氧化氮的机制增强GABA突触传递。L-精氨酸、NO 711和尼克酸作用之间的相似性表明,L-精氨酸抑制了一种GABA转运体。